Microwave-Assisted Chitosan-Functionalized Graphene Oxide as Controlled Intracellular Drug Delivery Nanosystem for Synergistic Antitumour Activity

被引:0
作者
Mengjun Shu
Feng Gao
Min Zeng
Chulang Yu
Xue Wang
Renhua Huang
Jianhua Yang
Yanjie Su
Nantao Hu
Zhihua Zhou
Ke Liu
Zhi Yang
Hongtao Tan
Lin Xu
机构
[1] Shanghai Jiao Tong University,Key Laboratory of Thin Film and Microfabrication (Ministry of Education), Department of Micro/Nano Electronics, School of Electronic Information and Electrical Engineering
[2] The First Affiliated Hospital of Harbin Medical University,Key Laboratory of Hepatosplenic Surgery (Ministry of Education), Department of General Surgery
[3] Shanghai Engineering Center for Visual Science and Photomedicine,Department of Ophthalmogy, Shanghai General Hospital (Shanghai First People’s Hospital), School of Global Health, Chinese Center for Tropical Diseases Research, Shanghai Jiao Tong University
[4] Center for Specialty Strategy Research of Shanghai Jiao Tong University China Hospital Development Institute,Department of Dermatology, Shanghai Ninth People’s Hospital, Affiliated To Shanghai Jiao Tong University School of Medicine
[5] Ningbo University,State Key Laboratory for Managing Biotic and Chemical Threats To the Quality and Safety of Agro
[6] Shanghai Jiao Tong University,Products, Key Laboratory of Biotechnology in Plant Protection of MOA and Zhejiang Province, Institute of Plant Virology
来源
Nanoscale Research Letters | / 16卷
关键词
Graphene oxide; Drug delivery; Adriamycin; Microwave-assisted reduction; Breast cancer; HER2; Trastuzumab;
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学科分类号
摘要
To achieve better antitumour efficacy, it is urgent to improve anticancer drug delivery efficiency in targeting cancer cells. In this work, chitosan-functionalized graphene oxide (ChrGO) nanosheets were fabricated via microwave-assisted reduction, which were employed to the intracellular delivery nanosystem for anticancer drug agent in breast cancer cells. Drug loading and release research indicated that adriamycin can be efficiently loaded on and released from the ChrGO nanosheets. Less drug release during delivery and better biocompatibility of ChrGO/adriamycin significantly improve its safety and therapeutic efficacy in HER2-overexpressing BT-474 cells. Furthermore, ChrGO/adriamycin in combination with trastuzumab exhibited synergistic antitumour activity in BT-474 cells, which demonstrated superior therapeutic efficacy compared with each drug alone. Cells treated with trastuzumab (5 μg/mL) or equivalent ChrGO/adriamycin (5 μg/mL) each elicited 54.5% and 59.5% cell death, respectively, while the combination treatment with trastuzumab and ChrGO/adriamycin resulted in a dramatic 88.5% cell death. The dual-targeted therapy displayed higher apoptosis, indicating superior therapeutic efficacy due to the presence of different mechanisms of action. The combined treatment of ChrGO/adriamycin and trastuzumab in BT-474 cells induced cell cycle arrest and apoptosis, which ultimately led to the death of augmented cancer cells. This work has provided a facile microwave-assisted fabrication of ChrGO as a controlled and targeted intracellular drug delivery nanosystem, which is expected to be a novel promising therapy for treating HER2-overexpressing breast cancer cells.
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